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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992685Generated: October 26, 2026

Triphenylphosphine → 4-(Benzoylthiomethyl)-1-methylpyrazole

https://huagongshe.com/reaction/992685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantPotassium BicarbonateHCID 516893—
Reactant(1-methyl-1H-pyrazol-4-yl)methanolHCID 11961423—
ReactantHCID 178526132HCID 178526132—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-(Benzoylthiomethyl)-1-methylpyrazoleHCID 18411601—

Reaction Steps

Under nitrogen atmosphere, 78.7 g of triphenylphosphine (300 m mol) and 47.2 ml of diethyl azodicarboxylate (300 m mol) were added to a stirred solution of 22.4 g of 4-hydroxymethyl-1-methylpyrazole (200 m mol) in THF (250 ml) at 5° C. After stirring for 1 hour at the same temperature, 42.3 ml of thiobenzoic acid (360 m mol) was added slowly to the mixture. The mixture was poured into a mixture of water and ethyl acetate, while Ph was adjusted to 9.5 with 30% potassium bicarbonate. Aqueous layer was separated, the organic layer was washed with brine, dried over magnesium sulfate. After filtration of the mixture, the filtrate was concentrated in vacuo, and the residue was purified on silica gel (eluent: n-hexane-ethyl acetate) to afford 4-(benzoylthiomethyl)-1-methylpyrazole (18.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06468995B1
Source datasetuspto-grants-2002_10
ORD IDord-1973982b4d134b29b792487866876acc
Source noteuspto-grants-2002_10